A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386077



Internal ID21043630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87205901..87209700hg38UCSC Ensembl
chr4:88127053..88130852hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121771
Samples
Known GenesKLHL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer